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Cross-reactive anti-PfCLAG9 antibodies in the sera of asymptomatic parasite carriers of Plasmodium vivax

机译:间日疟原虫无症状寄生虫携带者血清中的交叉反应抗PfCLAG9抗体

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摘要

The PfCLAG9 has been extensively studied because their immunogenicity. Thereby, the gene product is important for therapeutics interventions and a potential vaccine candidate. Antibodies against synthetic peptides corresponding to selected sequences of the Plasmodium falciparum antigen PfCLAG9 were found in sera of falciparum malaria patients from Rondônia, in the Brazilian Amazon. Much higher antibody titres were found in semi-immune and immune asymptomatic parasite carriers than in subjects suffering clinical infections, corroborating original findings in Papua Guinea. However, sera of Plasmodium vivax patients from the same Amazon area, in particular from asymptomatic vivax parasite carriers, reacted strongly with the same peptides. Bioinformatic analyses revealed regions of similarity between P. falciparum Pfclag9 and the P. vivax ortholog Pvclag7. Indirect fluorescent microscopy analysis showed that antibodies against PfCLAG9 peptides elicited in BALB/c mice react with human red blood cells (RBCs) infected with both P. falciparum and P. vivax parasites. The patterns of reactivity on the surface of the parasitised RBCs are very similar. The present observations support previous findings that PfCLAG9 may be a target of protective immune responses and raises the possibility that the cross reactive antibodies to PvCLAG7 in mixed infections play a role in regulate the fate of Plasmodium mixed infections.
机译:由于PfCLAG9具有免疫原性,因此已被广泛研究。因此,该基因产物对于治疗干预和潜在的疫苗候选者很重要。在巴西亚马逊州朗多尼亚的恶性疟疾患者血清中发现了针对与恶性疟原虫抗原PfCLAG9的选定序列相对应的合成肽的抗体。在半免疫和免疫无症状寄生虫携带者中发现的抗体滴度比在临床感染者中高得多,这证实了在巴布亚几内亚的原始发现。但是,来自同一亚马逊地区的间日疟原虫患者的血清,特别是来自无症状间日疟原虫携带者的血清,与相同的肽强烈反应。生物信息学分析揭示了恶性疟原虫Pfclag9和间日疟原虫直系同源物Pvclag7之间的相似区域。间接荧光显微镜分析表明,在BALB / c小鼠中引起的针对PfCLAG9肽的抗体与感染了恶性疟原虫和间日疟原虫的人红细胞(RBC)反应。寄生红细胞表面的反应模式非常相似。本观察结果支持以前的发现,即PfCLAG9可能是保护性免疫反应的靶点,并增加了在混合感染中针对PvCLAG7的交叉反应抗体在调节疟原虫混合感染命运中发挥作用的可能性。

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